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Checklist could cut risks in brain bleed surgery

NCT ID NCT07315048

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a nurse-led safety program using checklists can reduce complications in patients undergoing emergency surgery for a brain bleed (subarachnoid hemorrhage). 156 adults were randomly assigned to receive either standard nursing care or standard care plus the extra safety program. The program focused on spotting and preventing 12 high-risk problems, such as re-bleeding, high brain pressure, and infections. The goal was to see if this approach lowers the number of nursing-related adverse events within 30 days after surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
HFMEA-based nursing-risk programme
What this could lead to
If it works, this could make emergency brain-aneurysm surgery safer by preventing common complications like re-bleeding and infections.
What could go wrong
This is a small, single-center study testing a behavioral intervention, not a drug. Results may not apply to other hospitals or settings.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

156 people

The number who actually took part.

Started

Mar 2022

Finished

Apr 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. sSAH confirmed by head CT and/or CT angiography (CTA) or digital subtraction angiography (DSA), with identified intracranial aneurysm; 2. Age 18-75 years; 3. Time from onset to admission ≤72 hours; 4. Undergoing emergency surgical treatment (open aneurysm clipping or endovascular coiling); 5. Hunt-Hess grade I-V; 6. Patient or family consent to participate in the study with signed informed consent. Exclusion Criteria: 1. Traumatic subarachnoid hemorrhage; 2. Concurrent other intracranial diseases (e.g., brain tumors, arteriovenous malformations); 3. Severe cardiac, hepatic, or renal dysfunction; 4. Coagulation disorders; 5. History of psychiatric disorders or cognitive impairment; 6. Pregnancy or lactation; 7. Transfer to another hospital or treatment withdrawal.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • West China Hospital of Sichuan University

    Chengdu, Sichuan, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.